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NCT06305351 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of K-757 and K-833 in Overweight/Obese Patients With Type 2 Diabetes

A Phase 1 study, sponsored by Kallyope.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT06305351: Completed Phase 1 study, sponsored by Kallyope.

NCT06305351 is a Phase 1 study that has completed, run by Kallyope. The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT06305351, a Phase 1 study, has completed, sponsored by Kallyope.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

This is a multiple dose study to evaluate the safety, tolerability, PK, and PD of K-757 and K-833 when co-administered in overweight/obese patients with Type 2 diabetes mellitus (T2DM)

Interventions

  • DRUG K-757 and K-833 QD
  • DRUG K-757 and K-833 BID
  • DRUG Matching placebo to K-757 and K-833 QD
  • DRUG Matching placebo to K-757 and K-833 BID

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2023-12-07
Est. Completion 2024-06-21
Phase Phase 1
Kallyope

8 total trials

What the finished NCT06305351 record still lists

NCT06305351 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 4 interventions - of which K-757 and K-833 QD is the first listed.

NCT06305351 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06305351 about?

NCT06305351 is a clinical study titled "A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of K-757 and K-833 in Overweight/Obese Patients With Type 2 Diabetes". This is a multiple dose study to evaluate the safety, tolerability, PK, and PD of K-757 and K-833 when co-administered in overweight/obese patients with Type 2 diabetes mellitus (T2DM)

What is the current status of trial NCT06305351?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2023-12-07. Estimated completion is 2024-06-21.

What interventions are being tested in trial NCT06305351?

The interventions under investigation include: K-757 and K-833 QD (DRUG), K-757 and K-833 BID (DRUG), Matching placebo to K-757 and K-833 QD (DRUG), Matching placebo to K-757 and K-833 BID (DRUG).

Who is sponsoring clinical trial NCT06305351?

This trial is sponsored by Kallyope, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06305351's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06305351, the US trial registry maintained by the National Library of Medicine. NCT06305351 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.